Samsó Montserrat, Wagenknecht Terence, Allen P D
Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Nat Struct Mol Biol. 2005 Jun;12(6):539-44. doi: 10.1038/nsmb938. Epub 2005 May 22.
RyR1 is an intracellular calcium channel with a central role in muscle contraction. We obtained a three-dimensional reconstruction of the RyR1 in the closed state at a nominal resolution of approximately 10 A using cryo-EM. The cytoplasmic assembly consists of a series of interconnected tubular structures that merge into four columns that extend into the transmembrane assembly. The transmembrane assembly, which has at least six transmembrane alpha-helices per monomer, has four tilted rods that can be fitted with the inner helices of a closed K(+) channel atomic structure. The rods splay out at the lumenal side and converge into a dense ring at the cytoplasmic side. Another set of four rods emerges from this ring and shapes the inner part of the four columns. The resulting constricted axial structure provides direct continuity between cytoplasmic and transmembrane assemblies, and a possible mechanism for control of channel gating through conformational changes in the cytoplasmic assembly.
兰尼碱受体1(RyR1)是一种细胞内钙通道,在肌肉收缩中起核心作用。我们使用冷冻电子显微镜以约10埃的标称分辨率获得了处于关闭状态的RyR1的三维重建结构。胞质组件由一系列相互连接的管状结构组成,这些结构合并成延伸至跨膜组件的四列。跨膜组件每个单体至少有六个跨膜α螺旋,有四根倾斜的杆,可与封闭的钾离子通道原子结构的内部螺旋相匹配。这些杆在管腔侧展开,在胞质侧汇聚成一个致密环。另一组四根杆从这个环中伸出,塑造了四列的内部部分。由此产生的收缩轴向结构在胞质组件和跨膜组件之间提供了直接连续性,以及一种通过胞质组件构象变化控制通道门控的可能机制。